3-(2-morpholino-6-(quinolin-3-ylamino)pyrimidin-4-yl)phenol | 701244-03-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 3-(2-morpholino-6-(quinolin-3-ylamino)pyrimidin-4-yl)phenol
• 英文别名: 3-[2-morpholin-4-yl-6-(quinolin-3-ylamino)pyrimidin-4-yl]phenol
• CAS: 701244-03-3
• 化学式: C₂₃H₂₁N₅O₂
• 分子量: 399.452
• InChiKey: BQMIYSBHFVDQPF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  30
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  83.4
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  N-(6-bromo-2-morpholinopyrimidin-4-yl)quinolin-3-amine 、 3-羟基苯硼酸 在 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 sodium carbonate 作用下， 以 乙二醇二甲醚 、 水 为溶剂， 反应 0.17h， 生成 3-(2-morpholino-6-(quinolin-3-ylamino)pyrimidin-4-yl)phenol
  参考文献：
  名称：

  Synthesis and in Vitro and in Vivo Evaluation of Phosphoinositide-3-kinase Inhibitors

  摘要：

  Phospoinositide-3-kinases (PI3K) are important oncology targets due to the deregulation of this signaling pathway in a wide variety of human cancers. series of 2 morpholino, 4-substituted, 6-(3-hydroxyphenyl) pyrimidines have been reported as potent inhibitors of PI3Ks. Herein, we describe the structure guided optimization of these,pyrimidines with a focus on replacing the phenol moiety, while maintaining potent target inhibition and improving in vivo properties A series of 2-morpholino, 4-substituted, 6-heterocyclic pyrimidines, which potently inhibit PI3K, were discovered,Within-this series a compound, 17, Was identified with suitable pharmacokinetic (PK) properties, which allowed for the establishment of a PI3K PK/pharmacodynamic-efficacy relationship as determined by in vivo inhibition of AKT(Ser473) phosphorylation and tumor growth inhibition in a mouse A2780 tumor xenograft model.

  DOI：

  10.1021/ml1001932

文献信息

• SMALL MOLECULE PI 3-KINASE INHIBITORS AND METHODS OF THEIR USE
  申请人：Nuss John N.

  公开号：US20090060912A1

  公开（公告）日：2009-03-05

  Compounds having formula I are provided where the variables have the values described herein. Pharmaceutical formulations include the compounds or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable carrier and combinations with other agents. A method of treating a patient comprises administering a pharmaceutical formulation according to the invention to a patient in need thereof.

  提供了化学式I的化合物，其中变量具有所述的值。药物制剂包括该化合物或其药学上可接受的盐以及药学上可接受的载体和其他药物的组合。治疗患者的方法包括向需要该制剂的患者给予本发明的药物制剂。
• 2,4,6-trisubstituted pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer
  申请人：Novartis AG

  公开号：EP2316831A1

  公开（公告）日：2011-05-04

  Compounds having formula I are provided where the variables have the values described herein. Pharmaceutical formulations include the compounds or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable carrier and combinations with other agents. These compounds are phosphotidylinositol 3-kinase (PI3K) inhibitors.

  提供了具有式 I 的化合物，其中的变量具有本文所述的值。 药物制剂包括这些化合物或其药学上可接受的盐和药学上可接受的载体以及与其他制剂的组合。这些化合物是磷脂酰肌醇 3- 激酶（PI3K）抑制剂。
• 2,4,6-TRISUBSTITUTED PYRIMIDINES AS PHOSPHOTIDYLINOSITOL (PI) 3-KINASE INHIBITORS AND THEIR USE IN THE TREATMENT OF CANCER
  申请人：Novartis AG

  公开号：EP1575940B1

  公开（公告）日：2011-10-05
• 2-(morpholin-4-yl)pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer
  申请人：Novartis AG

  公开号：EP2316831B1

  公开（公告）日：2013-03-06
• US7423148B2
  申请人：——

  公开号：US7423148B2

  公开（公告）日：2008-09-09